Mcl-1 Interacts with Akt to Promote Lung Cancer Progression.


Journal

Cancer research
ISSN: 1538-7445
Titre abrégé: Cancer Res
Pays: United States
ID NLM: 2984705R

Informations de publication

Date de publication:
15 12 2019
Historique:
received: 20 03 2019
revised: 23 09 2019
accepted: 23 10 2019
pubmed: 31 10 2019
medline: 28 5 2020
entrez: 31 10 2019
Statut: ppublish

Résumé

Mcl-1 is a unique antiapoptotic Bcl2 family protein that functions as a gatekeeper in manipulating apoptosis and survival in cancer cells. Akt is an oncogenic kinase that regulates multiple cellular functions and its activity is significantly elevated in human cancers. Here we discovered a cross-talk between Mcl-1 and Akt in promoting lung cancer cell growth. Depletion of endogenous Mcl-1 from human lung cancer cells using CRISPR/Cas9 or

Identifiants

pubmed: 31662324
pii: 0008-5472.CAN-19-0950
doi: 10.1158/0008-5472.CAN-19-0950
pmc: PMC6911632
mid: NIHMS1541634
doi:

Substances chimiques

Antineoplastic Agents 0
MCL1 protein, human 0
Myeloid Cell Leukemia Sequence 1 Protein 0
Proto-Oncogene Proteins c-akt EC 2.7.11.1

Types de publication

Journal Article Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

6126-6138

Subventions

Organisme : NCI NIH HHS
ID : R01 CA200905
Pays : United States
Organisme : NCI NIH HHS
ID : P50 CA217691
Pays : United States
Organisme : NCI NIH HHS
ID : P30 CA138292
Pays : United States
Organisme : NCI NIH HHS
ID : R01 CA193828
Pays : United States
Organisme : NCI NIH HHS
ID : R01 CA136534
Pays : United States

Informations de copyright

©2019 American Association for Cancer Research.

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Auteurs

Guo Chen (G)

Department of Radiation Oncology, Emory University School of Medicine and Winship Cancer Institute of Emory University, Atlanta, Georgia.

Dongkyoo Park (D)

Department of Radiation Oncology, Emory University School of Medicine and Winship Cancer Institute of Emory University, Atlanta, Georgia.

Andrew T Magis (AT)

Institute for Systems Biology, Seattle, Washington.

Madhusmita Behera (M)

Department of Hematology and Medical Oncology, Emory University School of Medicine and Winship Cancer Institute of Emory University, Atlanta, Georgia.

Suresh S Ramalingam (SS)

Department of Hematology and Medical Oncology, Emory University School of Medicine and Winship Cancer Institute of Emory University, Atlanta, Georgia.

Taofeek K Owonikoko (TK)

Department of Hematology and Medical Oncology, Emory University School of Medicine and Winship Cancer Institute of Emory University, Atlanta, Georgia.

Gabriel L Sica (GL)

Department of Pathology and Laboratory Medicine, Emory University School of Medicine and Winship Cancer Institute of Emory University, Atlanta, Georgia.

Keqiang Ye (K)

Department of Pathology and Laboratory Medicine, Emory University School of Medicine and Winship Cancer Institute of Emory University, Atlanta, Georgia.

Chao Zhang (C)

Department of Biostatistics & Bioinformatics, Emory University School of Medicine and Winship Cancer Institute of Emory University, Atlanta, Georgia.

Zhengjia Chen (Z)

Department of Biostatistics & Bioinformatics, Emory University School of Medicine and Winship Cancer Institute of Emory University, Atlanta, Georgia.

Walter J Curran (WJ)

Department of Radiation Oncology, Emory University School of Medicine and Winship Cancer Institute of Emory University, Atlanta, Georgia.

Xingming Deng (X)

Department of Radiation Oncology, Emory University School of Medicine and Winship Cancer Institute of Emory University, Atlanta, Georgia. xdeng4@emory.edu.

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Classifications MeSH